Treatment Option
I recently was diagnosed with MAI in late August 2017.. This all started in May when I was admitted to the hospital for pneumonia. They found a spot on my lung, and I had to have a lung biopsy done in July. My pulmonologist put me on the Big 3(Clarithromycin, Ethambutol, Rifampin). I could not tolerate any of those medications so they had me stop all medications and referred me to an Infectious Disease doctor. Around 3 weeks ago infectious disease Dr. started me on Zithromax 500mg Daily. I have not noticed a change in my symptoms, and I am having more severe pains. I just turned 27 this month, and I am just disheartened because nothing seems to be helping. I had a flare up yesterday, and was put in observation. The only thing they tell me is to take pain medication, and may have to start me on nerve medicine. This is not something that I want. I have never taking medications in my life, and now all I do is try this medication or that..
I am just curious if anyone else have had similar issues.. I am just trying to find answers, thank you for taking the time for reading this.
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I had my first CT scan 3 years ago when I was first diagnosed with MAC. My second CT scan was last month. I had quite a number of chest X-rays in between. I have never been treated with antibiotics for MAC during these 3 years. I was given the option but decided not to and my pulmonary doctor agreed. The last CT scan and chest X-rays before that have not shown worsening of my lungs. In fact the last CT scan showed a slight improvement from 3 years ago. I don't have any breathing problems or fatigue. So still no drugs yet. I keep my fingers crossed I won't have to resort to them for the foreseeable future.
Hi Jkie: I took the big 3 for 2 years, on and off for 3. at first, just bad taste in mouth, tiredness, and nausea, which went away if I ate something. So it was pretty tolerable. But later on, it would start to hit my bowels, with hard core cramps. Also my vision got a lot worse and I got a wierd rash on my stomach. My heart beat harder. The reason I had to finally go off of them was because of the horrible cramping, loose bowels and too much weight loss.
@cowgirlmt, It is good to have a good support system. The love of family can help a lot too.
@jkiemen , Jo Ann, here are some guidelines for when you are put on the BIG 3: From Katherine's File Cabinet:
TESTING-baseline and periodic 1. Ethambutol – color vision and visual acuity: GET BASELINE PRIOR TO STARTING .. THEN QUARTERLY
2. Azithromycin – hearing and balance: GET BASELINE PRIOR TO STARTING .. THEN QUARTERLY
3. Rifampin - CBD (blood counts), liver and kidney function tests: GET BASELINE PRIOR TO STARTING .. THEN MONTHLY
OR TESTING:
BASELINE: HEARING AND VISION (Vision: Additional testing for eyes are use of the “eye chart” with letters read at 20 feet, and a red-green color book to distinguish changes in the ability to visualize colors.)
MONTHLY: BLOOD COUNTS, LIVER AND KIDNEY FUNCTION TESTS, SPUTUM CULTURES
QUARTERLY: HEARING and VISION
NOTE: Ethambutol – color vision and visual acuity – monthly ( Additional testing for eyes are use of the “eye chart” with letters read at 20 feet, and a red-green color book to distinguish changes in the ability to visualize colors.)
**** Lab tests:
CBC- Complete Blood Count (CBC)
ALT- Alanine Aminotransferase (ALT) LIVER
alk phosphatase- Alkaline Phosphatase - LIVER
serum creatinine-. Creatinine and Creatinine Clearance-SERUM CREATININE - KIDNEY
TESTING RECOMMENDED FOR VITAMIN LEVELS 1. Ask for your VD-3 level to be checked .. they can get too low. Speak to your Doctor first .. but I took: NATURE MADE brand 5,000 IU of Vitamin D-3 (NOT VD) *From our member @tdrell Terri, my Primary Dr at NJH
@cowgirlmt, Dear Kimmy, here are a few links that you might find interesting and helpful. https://www.nationaljewish.org/ntmvideos
https://www.youtube.com/watch?v=U1ZmJAQlgLw
https://www.youtube.com/watch?v=YeomndWSom8
@dmarks I took Clofazamine for about a year and the only side effects I noticed was that I had a nice tan (not the horrid purple skin you read about when you Google side effects) and also dry skin and dry eyes. I have been off MAC drugs since April 2017 with no residual side effects. I am one with cavitary lesions who decided against the surgery. I am well now and can always revisit it later if necessary.
Any guidelines to prevent nausea/diarrhea other than taking with food? like spacing them apart be several hours etc.